Evidence map›Paper›PMID 27470124›Full record

ArticleJournal of cellular and molecular medicine2016

Associations of polymorphisms in TXNIP and gene-environment interactions with the risk of coronary artery disease in a Chinese Han population.

Xue-Bin Wang, Ya-di Han, Shuai Zhang, Ning-Hua Cui, Ze-Jin Liu, Zhu-Liang Huang, Cong Li, Fang Zheng

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 31 citations in OpenAlex.

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  15. Oxidative Stress and the Kidney in the Space Environment.International journal of molecular sciences · 2018
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Xue-Bin WangCenter for Gene Diagnosis, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Ya-di HanCenter for Gene Diagnosis, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Shuai ZhangCenter for Gene Diagnosis, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Ning-Hua CuiDepartment of Clinical Laboratory, Children's Hospital of Zhengzhou, Zhengzhou, Henan, China.
Ze-Jin LiuCenter of Clinical Laboratory, Wuhan Asia Heart Hospital, Wuhan, Hubei, China.
Zhu-Liang HuangCenter for Gene Diagnosis, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Cong LiZhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Fang ZhengCenter for Gene Diagnosis, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Wuhan University · CNZhongnan Hospital of Wuhan University · CNSun Yat-sen University · CNWuhan Asia Heart Hospital · CNZhengzhou Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single nucleotide polymorphisms (SNPs) in thioredoxin-interacting protein (TXNIP) gene may modulate TXNIP expression, then increase the risk of coronary artery disease (CAD). In a two-stage case-control study with a total of 1818 CAD patients and 1963 controls, we genotyped three SNPs in TXNIP and found that the variant genotypes of SNPs rs7212 [odds ratio (OR) = 1.26, P = 0.001] and rs7211 (OR = 1.23, P = 0.005) were significantly associated with increased CAD risk under a dominant model. In haplotype analyses, compared with the reference haplotype, haplotype 'G-T' had a 1.22-fold increased risk of CAD (P = 0.003). We also observed the cumulative effects of SNPs rs7212 and rs7211 on CAD risk and the severity of coronary atherosclerosis. Moreover, the gene-environment interactions among the variant genotypes of SNP rs7212, smoking habit, alcohol drinking habit and history of type 2 diabetes were associated with a 3.70-fold increased risk of CAD (P < 0.001). Subsequent genotype-phenotype correlation analyses further observed the significant effects of SNP rs7212 on TXNIP mRNA expression, plasma TXNIP and malondialdehyde levels. Taken together, our data suggest that TXNIP SNPs may individually and cumulatively affect CAD risk through a possible mechanism for regulating TXNIP expression and gene-environment interactions.

Indexed as

Gene-Environment InteractionGenetic Association StudiesGenetic Predisposition to DiseaseAsian PeopleAtherosclerosisCarrier ProteinsCase-Control StudiesCoronary Artery DiseaseEthnicityGenes, DominantGenetic LociHaplotypesHumansMalondialdehydeModels, GeneticMultifactor Dimensionality ReductionCarrier ProteinsMalondialdehydeRNA, MessengerTXNIP protein, humanCAD riskgene-environment interactionsseverity of coronary atherosclerosisTXNIP expressionTXNIP SNPs

Identifiers

PMID27470124
PMCPMC5134401
OpenAlexW2511791867

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.